Label: BEACH GYPSY SPF-30- octinoxate, octocrylene, octisalate, avobenzone cream

  • NDC Code(s): 72085-146-04
  • Packager: MJ Products Association, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2023

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  • Drug Facts

  • ACTIVE INGREDIENTS

    Octinoxate 7.50%

    Octocrylene 7.00%

    Octisalate 4.00%

    Avobenzone 3.00%

    PURPOSE

    Sunscreen

  • USES

    • Helps prevent sunburn.
    • If used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.
  • WARNINGS

    • For external use only.

    Do not use

    on damaged or broken skin

    When using this product

    keep out of eyes. Rinse with water to remove.

    Stop use and consult physician

    if irritation or rash develops.

    Keep out of reach of children.

    If product is swallowed, get medical attention or contact poison control center immediately.

  • DIRECTIONS

    • Apply liberally 15 minutes before sun exposure. REAPPLY:
    • Al least every two-hours.
    • Immediately after swimming, sweating or towel drying. : Spending time in the sun increases your risk of skin cancer and early skin aging. To decreases this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including: SUN PROTECTION MEASURES
    • Limit time in the sun, especially between 10am and 2pm.
    • Wear long sleeve shirts, pants hats and sunglasses.
    • For children under 6 months, consult a physician.
  • OTHER INGREDIENTS

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Camellia Sinensis (Green Tea) Extract, Cetearyl Olivate, Cetyl Alcohol, Citric Acid, Cocos Nucifera (Coconut) Oil, Daucus Carota Sativa (Carrot) Seed Oil, Ethylhexylglycerin, Glitter: Regenerated Cellulose, FD&C Yellow #5, Aluminum; Glyceryl Stearate, Parfum (Fragrance), Phenoxyethanol, Polysorbate-20, Sorbitan Olivate, Tocopheryl Acetate (Vitamin E), Zemea (Corn) Propanedio.

  • OTHER INFORMATION

    Protect this product from excessive heat and direct sunlight.

  • QUESTIONS OR COMMENTS?

    Contact us directly at 1-888-601-0441

    Distr. by/par: Sunshine & Glitter

    MJ Products Association LLC

    9750 NW 17th Street

    Miami, FL 33172

    www.sunshineglitter.com

    All Rights Reserved.

  • Package Labeling

    Label0

  • INGREDIENTS AND APPEARANCE
    BEACH GYPSY SPF-30 
    octinoxate, octocrylene, octisalate, avobenzone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72085-146
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE40 mg  in 1 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    CARROT SEED OIL (UNII: 595AO13F11)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    REGENERATED CELLULOSE (UNII: BX81F82EWG)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    ALUMINUM (UNII: CPD4NFA903)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72085-146-04113 g in 1 TUBE; Type 0: Not a Combination Product03/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/01/2018
    Labeler - MJ Products Association, LLC (081022202)
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